Evidence map›Paper›PMID 24337378›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

Regulatory T cells shape the resident memory T cell response to virus infection in the tissues.

Jessica B Graham, Andreia Da Costa, Jennifer M Lund

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

73 citing papers in PubMed, 99 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Evolving role of CD8Frontiers in immunology · 2026
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Tissue-resident immune cells in the pathogenesis of multiple sclerosis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Review
  12. Review
  13. Article
  14. Keeping T cell memories in mind.Trends in immunology · 2022
    Review
  15. Article
  16. The dark side of Tregs during aging.Frontiers in immunology · 2022
    Review
  17. Review
  18. Article
  19. Article
  20. Article

13 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Jessica B GrahamVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109.
Andreia Da Costa
Jennifer M Lund
Cancer Research Center · USProgram for Appropriate Technology in Health · US

Funding

West Nile Virus and host control of innate defensesU19AI083019 · NIAID · UNIVERSITY OF WASHINGTON · PI CLARK, EDWARD A · 2009 to 2018
$22.5M
Diseases of Public Health Importance Training GrantT32AI007509 · NIAID · UNIVERSITY OF WASHINGTON · PI LUND, JENNIFER M · 1997 to 2024
$6.3M
Tissue Regulatory T Cells in Mucosal InfectionR01AI141435 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LUND, JENNIFER M · 2019 to 2023
$3.2M
Regulatory T cell Modulation of Immunity to Mucosal Viral InfectionsR01AI087657 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LUND, JENNIFER M · 2010 to 2014
$2.2M
NIAID NIH HHS R01 AI087657NIAID NIH HHS R01 AI141435NIAID NIH HHS T32 AI007509NIAID NIH HHS U19 AI083019
6 · The paper itself

Abstract

Regulatory T cells (Tregs) are well known for their role in dampening the immune responses to self-Ags and, thereby, limiting autoimmunity. However, they also must permit immune responses to occur against foreign infectious agents. Using a mouse model of West Nile virus infection, we examined the role of Tregs in the generation of effector and memory T cell responses in the secondary lymphoid organs, as well as the infected tissues. We found that Treg numbers and activation increased in both the secondary lymphoid organs and CNS postinfection. Using Foxp3(DTR) knock-in mice, we found that Treg-deficient mice had increased Ag-driven production of IFN-γ from both CD4(+) and CD8(+) T cells in the spleen and CNS during the effector phase. In mice lacking Tregs, there were greater numbers of short-lived effector CD8(+) T cells in the spleen during the peak of the immune response, but the memory CD8(+) T cell response was impaired. Specifically, we demonstrate that Treg-dependent production of TGF-β results in increased expression of CD103 on CD8(+) T cells, thereby allowing for a large pool of resident memory T cells to be maintained in the brain postinfection.

Indexed as

AnimalsAntigens, CDCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCentral Nervous SystemForkhead Transcription FactorsImmunologic MemoryIntegrin alpha ChainsInterferon-gammaMiceMice, Inbred C57BLSpleenT-Lymphocytes, RegulatoryTransforming Growth Factor betaWest Nile FeverWest Nile virusalpha E integrinsAntigens, CDForkhead Transcription FactorsFoxp3 protein, mouseIntegrin alpha ChainsInterferon-gammaTransforming Growth Factor beta

Identifiers

PMID24337378
PMCPMC3894741
OpenAlexW1908025802

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.